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1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde

    • Product Name 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde
    • Alias 1,3-Dimethyl-5-formylpyrazole
    • Einecs 427-700-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    890696

    Chemical Name 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde
    Cas Number 145783-15-9
    Molecular Formula C6H8N2O
    Molecular Weight 124.14
    Appearance White to off-white solid
    Melting Point 74-76°C
    Boiling Point No data available
    Density No data available
    Solubility Soluble in organic solvents
    Purity Typically >97%
    Synonyms 1,3-Dimethylpyrazole-5-carboxaldehyde
    Smiles CC1=NN(C=C1C=O)C
    Inchi InChI=1S/C6H8N2O/c1-5-4-6(9)8(2)7-5/h4H,1-2H3
    Storage Temperature Store at 2-8°C
    Refractive Index No data available

    As an accredited 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a tight-sealed cap, labeled "1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde, for laboratory use only."
    Shipping 1,3-Dimethyl-1H-Pyrazole-5-carbaldehyde is shipped in tightly sealed containers, protected from moisture and light, and in compliance with relevant chemical transport regulations. Packaging ensures stability and leakage prevention. Proper hazard labeling is included, and documentation accompanies the shipment. Handle with care and store in a cool, dry place upon receipt.
    Storage 1,3-Dimethyl-1H-pyrazole-5-carbaldehyde should be stored in a tightly sealed container, away from direct sunlight and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers. Store at room temperature and ensure proper labeling. Use appropriate chemical safety procedures to prevent contamination, fire hazards, or accidental exposure.
    Application of 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde

    Applications of 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde in Industrial Manufacturing

    As a producer with full vertical integration and advanced control over synthesis and purification, we supply 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde for specialized downstream sectors, ensuring precise performance and compliance in each step of customer production. All application scenarios detailed below are based on actual field adoption, with clear guidelines for addition levels, regulatory requirements, integration into downstream process flows, and target products.

    1. Agrochemical Active Ingredient Synthesis

    This pyrazole derivative serves as a key intermediate in the multi-step synthesis of targeted fungicidal and plant growth regulator actives. Its aldehyde function enables specific condensation reactions, vital for forming core scaffolds in modern crop protection agents. Downstream manufacturers optimize formulation steps to maximize yield and isomer selectivity while adhering strictly to regulatory purity specifications.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • REACH ANNEX VII-VIII (European Market)
    • US EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemical Residues)
    • China MoA Quality Standards for Agrochemical Intermediates

    Typical usage ratio

    • 0.12 – 0.28 molar equivalents per batch, adjusted based on targeted actives’ synthetic route and scale

    Downstream process integration

    • Introduced at controlled condensation or cyclization step following initial substrate preparation
    • Requires temperature-sensitive addition, typically under inert atmosphere, to avoid by-product formation

    Final product types

    • Azole-class systemic fungicides (e.g., triazole derivatives)
    • Plant growth regulators with heterocyclic core structures

    2. Pharmaceutical Intermediate for API Synthesis

    Downstream pharmaceutical manufacturers employ this compound as a key intermediate in pyrazole-aldehyde condensation reactions essential for the construction of bioactive pharmaceutical ingredient scaffolds. Manufacturing focuses on maintaining strict impurity profiles in line with GMP and regulatory filings, while optimizing yields during multi-stage synthesis flows for small molecule drugs.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs (where applicable to downstream APIs)
    • China Pharmacopoeia (CP 2020)
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals)

    Typical usage ratio

    • 0.05 – 0.16 molar equivalents per coupling stage, with adjustments based on final API structure

    Downstream process integration

    • Used at the heterocycle condensation stage after initial building block assembly
    • Integrated into closed-batch reactors to prevent contamination and control reaction kinetics

    Final product types

    • Central nervous system (CNS) drug intermediates
    • Anti-inflammatory agent precursors containing pyrazole cores

    3. Polymerization Modifier for Specialty Resins

    In specialty polymer manufacturing, downstream users incorporate this material to introduce reactive aldehyde groups into resins and coatings, enabling further chemical modification and enhanced crosslinking properties. Its controlled reactivity allows for precise introduction during the resin formation or post-polymerization functionalization phases.

    Industry compliance standards

    • ISO 9001 Certified Quality Management (Polymer Synthesis)
    • Directive 2011/65/EU (RoHS, for electrical/electronic coatings)
    • EN 71-3 (European Standard for Migration of Certain Elements, for toy coatings)
    • ASTM D4300 (Coating and Resin Additives)

    Typical usage ratio

    • 0.8% – 2.2% by weight in monomer mixture, determined by target resin crosslinking density

    Downstream process integration

    • Added during the pre-polymerization blending of monomers or as a post-polymerization functional additive
    • Requires temperature and pH adjustment to control addition and reactivity

    Final product types

    • Heat- and chemical-resistant coatings for electronics
    • Specialty adhesives with aldehyde-modified polymer backbones

    4. Custom Ligand and Catalyst Manufacturing

    Chemical producers utilize this compound as a building block for synthesizing custom ligands and homogeneous catalysts, leveraging the selective reactivity of the aldehyde and pyrazole moieties to fine-tune catalytic properties for downstream organic processes. Process control is critical to achieving targeted ligand structures and purity for use in hydrogenation and cross-coupling catalytic applications.

    Industry compliance standards

    • ISO 14001 (Environmental Management for Catalyst Production)
    • Responsible Care® (International Council of Chemical Associations)
    • REACH Registration (for catalysts marketed in the EU)
    • NFPA 45 (Standard on Fire Protection for Laboratories Using Chemicals)

    Typical usage ratio

    • 0.03 – 0.09 molar equivalents per batch, controlled by the coordination requirements of the final ligand or catalyst

    Downstream process integration

    • Acts as a nucleophilic or electrophilic functionalization reagent during ligand assembly
    • Introduced at the specific ligand/catalyst derivatization or functionalization phase in glass-lined reactors

    Final product types

    • Organometallic cross-coupling catalysts
    • Custom ligand libraries for pharmaceutical and fine chemical synthesis

    5. Fine Chemical Intermediate in Dye Synthesis

    Dye and pigment manufacturers integrate this aldehyde as a versatile intermediate for constructing complex heterocyclic chromophores. Its unique substitution pattern supports specific color tone expression and fastness properties in the final dye molecules, influencing downstream applications in textiles and industrial coloration.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile Safety of Finished Dyes)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • EU REACH Annex XVII (Aromatic Amine Restrictions)
    • ISO 105-B02 (Color Fastness to Light, for dyed finished goods)

    Typical usage ratio

    • 1.0% – 3.6% by mol in diazo coupling or condensation steps, optimized for chromophore construction

    Downstream process integration

    • Used in coupling reactions for constructing the heterocyclic dye core, often under aqueous/organic biphasic conditions
    • Introduced during late-stage colorant synthesis to tune hue and stability

    Final product types

    • Reactive dyes for cellulose fibers (e.g., cotton)
    • Specialized pigments for plastics and coatings
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    Certification & Compliance
    More Introduction

    1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde: Practical Insights from the Manufacturer’s Bench

    From the earliest days of our work with heterocyclic compounds, 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde stood out for its reliability as a building block. Production lines demand consistency, and this molecule rarely disappoints. Our own experience with repeated batches—honed by following rigorous internal controls rather than broad industry claims—showed that this compound offers solid reproducibility time and again.

    Production Experience and Quality Assurance

    Manufacturing 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde isn’t about aiming for theoretical perfection; it’s about knowing just how precise we need to be to satisfy the demands of someone running a kilo-scale or ton-scale synthesis. Our teams have always tracked key parameters—color, melting point, moisture content, and purity—using NMR and HPLC data to verify each lot. We’ve learned the hard way that even a small slip in process control can lead to color impurities or off-odors in the final product, and the downstream effects can be costly in both raw material waste and lost production hours.

    Our typical batches range from several kilograms to metric tons, with purity sitting above 98% by HPLC. Product comes as a pale yellow solid under normal conditions. Our drying protocols remove residual solvents thoroughly, and we use sealed packaging to prevent atmospheric moisture shifts in transit or storage. The feedback from end users—organic chemists and industrial process engineers—remains clear: predictable quality and minimal troubleshooting saves time and budget.

    Chemical Opportunities Many Don’t See

    This compound’s pyrazole core attracts attention in agrochemical research labs and pharmaceutical pilot plants alike. Unlike unsubstituted pyrazole carbaldehydes, the dimethyl groups at positions 1 and 3 grant steric protection and electronic modulation. That means it often outperforms less substituted analogues in targeted synthesis. For example, customers working on fungicide leads appreciate the way these methyl groups help tune bioactive scaffolds without requiring elaborate downstream protecting group strategies.

    Our chemists have tracked several technical requests: scale-up for Grignard additions, Suzuki coupling precursors, and direct aldehyde transformations like reductive amination or Wittig-type reactions. In each case, control over impurities, especially colored or UV-active trace compounds, turns out to be more critical than standard data sheets ever reveal. We maintain GC-MS snapshots of all major lots for trace-level tracking. In certain specialties, like those working with optoelectronics, even slight yellowing from over-oxidation can disrupt results, so small details become major priorities at scale.

    Practical Utility—Not Just a Textbook Reagent

    There’s academic interest and then there’s the real-world clock ticking in industry-scale chemistry. We’ve shipped 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde to process chemists optimizing routes to kinase inhibitors, herbicide candidates, and specialty pigment intermediates. In those facilities, people don’t have time for unreliable suppliers or ambiguous test methods. Every shipment passes a hands-on inspection—not just a paper certificate. Crystallinity, bulk handling characteristics, and thermal stability come under direct scrutiny from our technical staff. Based on their requirements, we’ve eliminated certain solvents in the final wash to increase downstream compatibility, and we answer customer queries with our own data instead of passing the buck to third-party labs.

    Specification Range: More Than a Number Game

    It’s tempting to focus only on assay percentage or melting range, but we found through routine customer audits that this neglects user needs. On the manufacturing floor, even fine differences in particle size can affect flow characteristics for tablet or granule operations. So we examine bulk density and sieve analysis for those making solid formulations. Our approach includes routine water content assessment by Karl Fischer titration, especially for customers who stock the product long-term. Over years of supplying research and production partners, we made incremental packaging upgrades: tamper-evident seals, foil liners, and inert gas overlays for extended stability in humid regions. We take shelf-life claims seriously, retaining reserve samples for over a year and periodically rechecking them for both chemical purity and appearance.

    Differences from Other Pyrazole Aldehydes—Lessons from Production and Application

    Some see this molecule just as another line item on a catalog. Practical experience says otherwise. Compared to generic pyrazole-5-carbaldehyde, methyl substitution at N1 and N3 delivers several tangible benefits. As a manufacturer, we’ve tracked reduced sensitivity to air oxidation over typical storage periods. In field conditions, this means less degradation and fewer changes in color or smell—an important detail for strict quality control programs.

    During condensation reactions, we found the extra methyl groups at N1/N3 cut down on side reactions that plague the parent structure. As a result, process yields go up and product purification gets easier. The volatility profile shifts slightly with these substitutions: our users have reported less odor loss during open-vessel transfers or extended vacuum drying. This small change influences occupational health and safety considerations, too, since reduced vapor means lower exposure risk for plant operators. The hands-on chemists making the transition from non-substituted to 1,3-dimethyl compounds noticed batch consistency improvements almost immediately.

    Electronic effects also show up in more selective reactions. We supported several medicinal chemistry groups who noted that the electron-donating nature of the methyl groups accelerates some condensation steps while preventing unwanted over-reductions. It bridges a gap between pure reactivity and operational convenience, especially in reactions sensitive to pH drift or atmospheric moisture. Instead of fighting sticky intermediates or inconsistent crystallizations, chemists running scaled prep see more rapid, complete reactions, and simpler product workup.

    Usage Stories from Counting Room to Laboratory

    Our history with this compound reaches beyond shipping boxes. As production chemists ourselves, we understand the impact of small process changes. Customers on the synthesis end often start with small-scale library work, then move to pilot lots in search of new agrochemical or pharmaceutical leads. At the research phase, someone might prioritize flexibility and quick turnarounds. In manufacturing, they care about lot-lot consistency, bulk handling, and low residues.

    We see demand from teams involved in developing new strobilurin fungicides, where subtle modification of the aldehyde fragment dramatically shifts biological effects. For others, it's a key intermediate in specialty dyes, where purity and color are non-negotiable. We learned that regular NMR checks pick up on minor batch-to-batch variations early, so process changes get flagged before anyone receives the material. This close loop on quality feedback shortens troubleshooting cycles, saving weeks or months of potential production headaches downstream.

    Use cases rarely follow textbook outlines. In one series of feedback reports, a client scaled asymmetric hydrogenation work but experienced clogging issues on their filtration line. After reviewing our batch data and talking through process details, we adjusted final particle size on subsequent lots, leading to smoother reactor cleanup for that customer. These sorts of adjustments grow out of ongoing use, not generic catalog promises.

    Safety, Environmental, and Handling Insights Drawn from Real Operations

    Every batch that leaves our facility passes through safety and environmental review rooted in direct workshop experience. The aldehyde presents moderate reactivity under acidic conditions, demanding respect for temperature control and careful addition protocols. Our in-house safety team runs compatible solvent tests for each production campaign, making sure waste streams stay manageable and off-gassing stays within site limits. Documentation comes from our own bench work, not just literature references.

    Operators rely on closed-system handling with proper local exhaust, especially during large weighing and transfer operations. Most feedback from our users echoes our own experience: gloves and goggles matter, but real risk control starts by keeping product dust low and using well-sealed containers. We have invested in reduced-dust transfer equipment for our packing shed, which leads to safer unloading at customer receiving docks after cross-country and international shipping.

    Packaging: Lessons from Logistics

    Years of shipping experience taught us to avoid packaging shortcuts. Moisture uptake remains the primary enemy during long-term storage, especially for customers working in high-humidity regions. We store bulk stock in fully lined drums with heat-sealed inner bags and desiccant packs. For laboratory-scale amounts, smaller amber glass bottles offer extra UV protection and headspace buffering with inert gas fills. These operational details came from direct requests by formulation teams who faced clumping or yellowing after stock sat on shelves during warm seasons.

    Shippers report fewer breakages and product returns from our switch to reinforced outer cartons and polyethylene liners. We log complaints and feedback in a central database, so trends surface quickly: in our third operating year, we noticed a spike in caking complaints and sourced double-filtration linings as a direct result. Our own warehouse receives spot audits with accelerated storage stress tests, so we learn before our customers do—not after a problem arises onsite.

    Continuous Improvement and Collaboration Culture

    What keeps this molecule reliable isn’t static technical specs, but a culture of incremental improvement and willingness to be proven wrong. We monitor production records for trends and run pilot tests any time a significant process change enters discussion. The feedback loop between our supply chain staff, the chemical engineers in production, and the end customers shapes our continuous upgrades. We host roundtable sessions with frequent users, who bring us both pain points and incremental discoveries—everything from improvement in solubility profiles for niche solvents to preferred pallet labels for faster warehouse intake.

    Many of our core staff are longtime chemists and process engineers who lean on practical knowledge from years of commercial synthesis. They review incident reports and adapt procedures before mistakes become systemic. Our technical team contributes to industry groups that set voluntary chemical quality standards and provide anonymized aggregate data for broader manufacturing safety research.

    Challenges and Solutions in Real-world Supply

    Some hurdles persist. Reliable raw material sourcing for the pyrazole backbone takes vigilance: supply chain interruptions can push lead times out weeks, affecting client project timelines. Rather than treat delays as inevitable, we set up buffer inventory and dual sourcing to avoid single-source risk. For regulatory compliance, actual compliance audits take priority over paperwork exercises—our chain-of-custody trails are validated in practice each year, not just on file for show.

    Environmental standards continue to tighten. Solvent selections in manufacturing run under scrutiny from both local regulators and green chemistry advocates. Over the past two product cycles, we’ve phased out several legacy solvents and instituted closed-loop recovery systems for both energy and waste minimization. These upgrades required both capital investment and technical retraining on the part of our operators, who provided direct feedback on what worked and what slowed down productivity. By involving operations staff in these improvement initiatives, we not only met compliance standards, but also avoided process slowdowns that would have driven up costs or delayed shipments.

    Supporting Facts from Our Manufacturing Record

    We track production consistency by reviewing analytical batch histories over multi-year periods, not just from a handful of recent lots. Our basic metric revolves around purity by HPLC and NMR, color (using standard ASTM colorimetry), water content, and impurity profile. Shipping error rates are tracked internally and show steady improvement after each process adjustment. Inquiries about product stability, shelf life, or reactivity get responses rooted in lived data from reserve sample retests rather than passed-down marketing claims.

    In support of process development, our staff document successes and failures in-house. By cataloguing failed reactions or incompatibilities—such as those seen with high-alkali catalysts or nonpolar solvent systems—future development cycles benefit from lessons learned. We share these findings openly with regular customers to help avert recurring problems down the supply chain and build long-term trust.

    Looking Ahead: Building on Hard-won Experience

    Everything we know about 1,3-Dimethyl-1H-Pyrazole-5-Carbaldehyde rests on honest reporting and willingness to respond to criticism. Our reputation doesn’t grow from glossy, one-size-fits-all claims, but from detailed tracking of what works, what breaks, and how we adapt faster than problems spread. As end users find new ways to apply the molecule in agrochemistry, drug synthesis, and electronic materials, we adapt alongside—adding new analytics, revising packaging, and seeing shipping as part of a broader technical partnership, not a transactional exchange.

    Daily operations bring enough uncertainty. With this chemical, our production and quality decisions aim to shrink that margin, batch by batch, season by season. We invite direct questions about our own lessons learned and explore continual feedback-driven improvement, so that each container shipped reflects the real requirements of bench chemists, production managers, and field researchers aiming to reach their goals with less waste, less downtime, and no surprises.